ENST00000369458.8:c.835C>T
MANE Select
|
ENSP00000358470.3:p.Leu279=
|
|
ENST00000328189.7:c.487C>T
|
ENSP00000328168.3:p.Leu163=
|
|
ENST00000359008.8:c.844C>T
|
ENSP00000351899.4:p.Leu282=
|
|
ENST00000369458.7:c.835C>T
|
ENSP00000358470.3:p.Leu279=
|
|
ENST00000539893.5:c.550C>T
|
ENSP00000444724.1:p.Leu184=
|
|
NM_001253849.1:c.550C>T
|
NP_001240778.1:p.Leu184=
|
|
NM_001253850.1:c.487C>T
|
NP_001240779.1:p.Leu163=
|
|
NM_024626.3:c.835C>T
|
NP_078902.2:p.Leu279=
|
|
NR_045603.1:n.1030C>T
|
|
|
NR_045604.1:n.734C>T
|
|
|
XM_011542143.1:c.886C>T
|
XP_011540445.1:p.Leu296=
|
|
XM_011542144.1:c.889C>T
|
XP_011540446.1:p.Leu297=
|
|
XM_011542145.1:c.850C>T
|
XP_011540447.1:p.Leu284=
|
|
XM_011542143.2:c.985C>T
|
XP_011540445.2:p.Leu329=
|
|
XM_017002335.2:c.850C>T
|
XP_016857824.1:p.Leu284=
|
|
NM_024626.4:c.835C>T
MANE Select
|
NP_078902.2:p.Leu279=
|
|
NR_045603.2:n.997C>T
|
|
|
NR_045604.2:n.701C>T
|
|
|
NM_001253849.2:c.550C>T
|
NP_001240778.1:p.Leu184=
|
|
NM_001253850.2:c.487C>T
|
NP_001240779.1:p.Leu163=
|
|